4-Bromo-3-fluoro-5-methoxypyridine

98%

Reagent Code: #155017
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CAS Number 1256825-73-6

science Other reagents with same CAS 1256825-73-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 2061 g/mol
Formula C₆H₅BrFNO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug candidates. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce functionalized pyridine moieties into target compounds. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-withdrawing properties and structural stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿22,200.00
250mg
10-20 days ฿37,720.00
4-Bromo-3-fluoro-5-methoxypyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug candidates. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce functionalized pyridine moieties into target compounds. Also utilized in agrochemical research for designing novel pesticides a

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its halogenated pyridine structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex drug candidates. Commonly employed in Suzuki and Buchwald–Hartwig reactions to introduce functionalized pyridine moieties into target compounds. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-withdrawing properties and structural stability.

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